Canonical Allele Identifier: CA2259725167
Gene: KRT10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40818891_40819035delinsGCCGGAGCTGCCGCCCCCGTAGCCGCCGCCGCCGCCGCCGGAACTGCCACCACCGTAGCCGCCGCTGGAACTGCCGCCGTGGCCGCCGCTGGAGCTTCCGCCCCCGTAGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCT , CM000679.2:g.40818891_40819035delinsGCCGGAGCTGCCGCCCCCGTAGCCGCCGCCGCCGCCGCCGGAACTGCCACCACCGTAGCCGCCGCTGGAACTGCCGCCGTGGCCGCCGCTGGAGCTTCCGCCCCCGTAGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCT GRCh38
NC_000017.10:g.38975143_38975287delinsGCCGGAGCTGCCGCCCCCGTAGCCGCCGCCGCCGCCGCCGGAACTGCCACCACCGTAGCCGCCGCTGGAACTGCCGCCGTGGCCGCCGCTGGAGCTTCCGCCCCCGTAGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCT , CM000679.1:g.38975143_38975287delinsGCCGGAGCTGCCGCCCCCGTAGCCGCCGCCGCCGCCGCCGGAACTGCCACCACCGTAGCCGCCGCTGGAACTGCCGCCGTGGCCGCCGCTGGAGCTTCCGCCCCCGTAGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCT GRCh37
NC_000017.9:g.36228669_36228813delinsGCCGGAGCTGCCGCCCCCGTAGCCGCCGCCGCCGCCGCCGGAACTGCCACCACCGTAGCCGCCGCTGGAACTGCCGCCGTGGCCGCCGCTGGAGCTTCCGCCCCCGTAGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCT NCBI36
NG_008405.1:g.8577_8721delinsAGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCTACGGGGGCGGAAGCTCCAGCGGCGGCCACGGCGGCAGTTCCAGCGGCGGCTACGGTGGTGGCAGTTCCGGCGGCGGCGGCGGCGGCTACGGGGGCGGCAGCTCCGGC
NG_033147.1:g.4800_4944delinsGCCGGAGCTGCCGCCCCCGTAGCCGCCGCCGCCGCCGCCGGAACTGCCACCACCGTAGCCGCCGCTGGAACTGCCGCCGTGGCCGCCGCTGGAGCTTCCGCCCCCGTAGCCGCCGCCGGAGCTTCCGCCGCCGGAGCTTCCGCCT

Transcript Alleles

HGVS Amino-acid change
ENST00000269576.6:c.1500_1644delinsAGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCTACGGGGGCGGAAGCTCCAGCGGCGGCCACGGCGGCAGTTCCAGCGGCGGCTACGGTGGTGGCAGTTCCGGCGGCGGCGGCGGCGGCTACGGGGGCGGCAGCTCCGGC MANE Select ENSP00000269576.5:p.Gly500=
ENST00000635956.2:c.1500_1644delinsAGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCTACGGGGGCGGAAGCTCCAGCGGCGGCCACGGCGGCAGTTCCAGCGGCGGCTACGGTGGTGGCAGTTCCGGCGGCGGCGGCGGCGGCTACGGGGGCGGCAGCTCCGGC ENSP00000490524.2:p.Gly500=
ENST00000269576.5:c.1500_1644delinsAGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCTACGGGGGCGGAAGCTCCAGCGGCGGCCACGGCGGCAGTTCCAGCGGCGGCTACGGTGGTGGCAGTTCCGGCGGCGGCGGCGGCGGCTACGGGGGCGGCAGCTCCGGC ENSP00000269576.5:p.Gly500=
NM_000421.3:c.1500_1644delinsAGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCTACGGGGGCGGAAGCTCCAGCGGCGGCCACGGCGGCAGTTCCAGCGGCGGCTACGGTGGTGGCAGTTCCGGCGGCGGCGGCGGCGGCTACGGGGGCGGCAGCTCCGGC NP_000412.3:p.Gly500=
XM_005257343.2:c.1500_1644delinsAGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCTACGGGGGCGGAAGCTCCAGCGGCGGCCACGGCGGCAGTTCCAGCGGCGGCTACGGTGGTGGCAGTTCCGGCGGCGGCGGCGGCGGCTACGGGGGCGGCAGCTCCGGC XP_005257400.1:p.Gly500=
XM_005257343.3:c.1500_1644delinsAGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCTACGGGGGCGGAAGCTCCAGCGGCGGCCACGGCGGCAGTTCCAGCGGCGGCTACGGTGGTGGCAGTTCCGGCGGCGGCGGCGGCGGCTACGGGGGCGGCAGCTCCGGC XP_005257400.1:p.Gly500=
NM_000421.4:c.1500_1644delinsAGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCTACGGGGGCGGAAGCTCCAGCGGCGGCCACGGCGGCAGTTCCAGCGGCGGCTACGGTGGTGGCAGTTCCGGCGGCGGCGGCGGCGGCTACGGGGGCGGCAGCTCCGGC NP_000412.3:p.Gly500=
NM_000421.5:c.1500_1644delinsAGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCTACGGGGGCGGAAGCTCCAGCGGCGGCCACGGCGGCAGTTCCAGCGGCGGCTACGGTGGTGGCAGTTCCGGCGGCGGCGGCGGCGGCTACGGGGGCGGCAGCTCCGGC MANE Select NP_000412.4:p.Gly500=
NM_001379366.1:c.1500_1644delinsAGGCGGAAGCTCCGGCGGCGGAAGCTCCGGCGGCGGCTACGGGGGCGGAAGCTCCAGCGGCGGCCACGGCGGCAGTTCCAGCGGCGGCTACGGTGGTGGCAGTTCCGGCGGCGGCGGCGGCGGCTACGGGGGCGGCAGCTCCGGC NP_001366295.1:p.Gly500=